Tratado de limites das conquistas entre os muito altos, e poderosos senhores D. João V, Rey de Portugal, e D. Fernando VI, Rey de Espanha, pelo qual abolida a demarcação da linha meridiana, ajustada no Tratado de Tordesilhas de 7 de junho de 1494, se determina individualmente a raya dos domínios de huma e outra corôa na America Meridional :a de Portugal renuncia o direito, que allegava ter das Ilhas Filippinas, pelo dito Tratado de Tordesilhas, e pela escritura de Saragoça de 22 de abril de 1529 ; e cede a Espanha a Colonia do Sacramento, e o Territorio da margem septentrional do Rio da Prata, que lhe pertencia pelo Tratado de Utrecht de 6 de fevereiro de 1715, como também a Aldea de S. Christóvão, e terras adjacentes, que tinhão occupado os portuguezes entre os rios Japurá, e Isa, que desaguão no das Amazonas; a de Espanha renuncia todo o direito, que pelo dito Tratado de Tordesilhas allegava ter as terras possuidas pelos portuguezes na America Meridional ao Occidente da Linha Meridiana, ajustada naquelle Tratado ; e cede a Portugal todas as terras, e povoações da margem oriental do rio Uruguay, desde o rio Ibicuí para o norte, e a aldea de Santa Rosa, e outra qualquer estabelecida pelos espanhoes na margem oriental do rio Guaporé; com os plenos-poderes, e ratificações dos dous Monarchas, assignado em Madrid a 13 de janeiro de 1750

Referência: Diccionario Bibliographico Portuguez / Innocencio Francisco da Silva, 1862. v. 7, p. 386.

Elementos de desenho, e pintura : e regras geraes de perspectiva : dedicadas ao Senhor Rey D. João VI

O autor trabalhou a serviço da Duquesa de Cadaval em Lisboa, passando para o Brasil, foi nomeado professor de desenho da Aula Militar do Rio de Janeiro. Sobre o livro diz Inocêncio: "...segundo avaliador competente, é tida por 'um montão de absurdos, e não abona a perícia de Stockler nas bellas-artes...".

Tratado definitivo de paz, e união entre os serenissimos, e potentissimos Principes D. Joseph I. Rey Fidelissimo de Portugal, e dos Algarves, Jorge III, Rey da Gram Bretanha, de huma parte, Luiz XV, Rey Christianissimo de França, e D. Carlos III, Rey Catholico de Hespanha, da outra parte assignado em Pariz a dez de fevereiro de mil setecentos sessenta e tres :como plenos poderes, e ratificaçoens dos quatro monarcas contratantes, ajustando-se os actos que se passarão no dia 9 de março do mesmo anno, em que as ditas ratificações forão trocadas na mesma Corte de Pariz

Na Europa Central, onde ocorreram as principais batalhas terrestres, chamou-se Guerra dos Sete Anos; na Inglaterra, que foi a principal vencedora, chamou-se A Grande Guerra do Império; Nos Estados Unidos e no Canadá, que passou a ser inglês ao final dos combates, chamou-se de Guerra Franco-Índia.

Real cedula de S.M. y señores del Consejo : por la qual se manda observar, guardar y cumplir el Tratado de Paz y Amistad concluido entre el Rey Nuestro Señor y el Principe Regente de Portugal

Com certificado de cópia original.

Tratado em que se reconhece a Felipe 5º. por Rey de Hespanha

Exemplar manuscrito em caligrafia do século XVIII.

Análise do Anexo I do Decreto nº 8.456/2015 relativa às despesas da área temática IV – MCTI, MEC, MinC e ME

Analisa e detalha as ações orçamentárias das dotações iniciais constantes da Lei Orçamentária para 2015 – LOA 2015 dos órgãos integrantes da Área Temática IV (Ministério da Ciência, Tecnologia e Inovação – MCTI, Ministério da Educação – MEC, Ministério da Cultura – MinC e Ministério do Esporte – ME) que foram objeto de limitação de movimentação e empenho em face do Decreto nº 8.456, de 22 de maio de 2015.

Las Luces y el otro: ambigüedad del discurso ilustrado en torno al "Negro" en la Francia del siglo XVIII

Antonio Duplá Ansuategui, Piedad Frías Nogales e Iban Zaldúa (editores)

Prognostic Role of Host Cyclooxygenase and Cytokine Genotypes in a Caucasian Cohort of Patients with Gastric Adenocarcinoma

11 p.

Cartas enviadas por Enrique Areilza a Justo Garate entre 1924 y 1925

3 cartas (manuscritas) ; entre 210x215mm y 250x207mm. Caja 1 - Carpeta 44

Expression and activity profiles of DPP IV/CD26 and NEP/CD10 glycoproteins in the human renal cancer are tumor-type dependent

Background: Cell-surface glycoproteins play critical roles in cell-to-cell recognition, signal transduction and regulation, thus being crucial in cell proliferation and cancer etiogenesis and development. DPP IV and NEP are ubiquitous glycopeptidases closely linked to tumor pathogenesis and development, and they are used as markers in some cancers. In the present study, the activity and protein and mRNA expression of these glycoproteins were analysed in a subset of clear-cell (CCRCC) and chromophobe (ChRCC) renal cell carcinomas, and in renal oncocytomas (RO). Methods: Peptidase activities were measured by conventional enzymatic assays with fluorogen-derived substrates. Gene expression was quantitatively determined by qRT-PCR and membrane-bound protein expression and distribution analysis was performed by specific immunostaining. Results: The activity of both glycoproteins was sharply decreased in the three histological types of renal tumors. Protein and mRNA expression was strongly downregulated in tumors from distal nephron (ChRCC and RO). Moreover, soluble DPP IV activity positively correlated with the aggressiveness of CCRCCs (higher activities in high grade tumors). Conclusions: These results support the pivotal role for DPP IV and NEP in the malignant transformation pathways and point to these peptidases as potential diagnostic markers.

Ekonomian lizentziaturako matematika IV. Azterketak

Ekonomian Lizentziaturako Matematika IV irakasgaia gainditu behar duten ikasleentzat, eta baita ere, gai batzuetan, gradu berriko Matematika I eta Matematika II irakasgaiko ikasleentzat.Ekonomian Lizentziaturako Matematika IV irakasgaiko azken hamar urteetan jarri diren azterketak eta haien erantzunak aurkituko dituzue. Lehenengo zatian, egin gabeko azterketak daude, ordena kronologikoan, zaharrenetik berrienera, eta bigarren zatian, erantzunak daude, ordena kronologikoan ere baina gaika ere. Horrela, programaren gai bakoitzaren ariketa guztiak elkarrekin aurkituko dituzue, gaiz gai ikasi nahi izanez gero.

Annaes do Parlamento Brazileiro. Tomo IV [1878]

Anais do Parlamento Brasileiro, 1878.

[Reseña] F. Petrarca, De viris illustribus, I, II, IV (eds. S. Ferrone, C. Malta, P. de Capua), Firenze, Le Lettere, 2006-2007

[ES] Un real decreto de 1904, emitido con motivo de la celebración del VI Centenario del nacimiento de Petrarca (1304-1374), creó la Commissione per l’Edizione Nazionale delle Opere di Francesco Petrarca. Después de un siglo en el que los estudios petrarquescos han experimentado un florecimiento espectacular, con varias revistas y colecciones dedicadas exclusivamente a Petrarca y con una deslumbrante nómina de especialistas, han visto la luz siete de los veinte volúmenes previstos inicialmente.

Zur Verbreitung der einzelnen Altersklassen des Köhlers, Pollachius virens (L.), in der nördlichen Nordsee (ICES-Div. IV a)

The distribution was studied by analysing the catches during four research vessel cruises in summer and eight cruises in winter in the period 1985 - 1993. The emmigration of young saithe, spending the larval and first juvenil stages in the inshore waters of Norway and Scotland, starts during the summer in an age of two years.

Ancillary ligand effects : from zirconium(IV)-catalyzed homogeneous propylene polymerization to platinum(II)-mediated C-H bond activation

A series of C_s- and C₁-symmetric doubly-linked ansa-metallocenes of the general formula {1,1'-SiMe₂-2,2'-E-('ƞ⁵-C₅H₂-4-R¹)-(ƞ⁵-C₅H-3',5'-(CHMe₂)₂)}ZrC₂ (E = SiMe₂ (1), SiPh₂ (2), SiMe₂ -SiMe₂ (3); R¹ = H, CHMe₂, C₅H₉, C₆H₁₁, C₆H₅) has been prepared. When activated by methylaluminoxane, these are active propylene polymerization catalysts. 1 and 2 produce syndiotactic polypropylenes, and 3 produces isotactic polypropylenes. Site epimerization is the major pathway for stereoerror formation for 1 and 2. In addition, the polymer chain has slightly stronger steric interaction with the diphenylsilylene linker than with the dimethylsilylene linker. This results in more frequent site epimerization and reduced syndiospecificity for 2 compared to 1.

C₁-Symmetric ansa-zirconocenes [1,1 '-SiMe₂-(C₅H₄)-(3-R-C₅H₃)]ZrCl₂ (4), [1,1 '-SiMe₂-(C₅H₄)-(2,4-R₂-C₅H₂)]ZrCl₂ (5) and [1,1 '-SiMe₂-2,2 '-(SiMe₂-SiMe₂)-(C₅H₃)-( 4-R-C₅H₂)]ZrCl₂ (6) have been prepared to probe the origin of isospecificity in 3. While 4 and 3 produce polymers with similar isospecificity, 5 and 6 give mostly hemi-isotactic-like polymers. It is proposed that the facile site epimerization via an associative pathway allows rapid equilibration of the polymer chain between the isospecific and aspecific insertion sites. This results in more frequent insertion from the isospecific site, which has a lower kinetic barrier for chain propagation. On the other hand, site epimerization for 5 and 6 is slow. This leads to mostly alternating insertion from the isospecific and aspecific sites, and consequently, a hemi-isotactic-like polymers. In comparison, site epimerization is even slower for 3, but enchainment from the aspecific site has an extremely high kinetic barrier for monomer coordination. Therefore, enchainment occurs preferentially from the isospecific site to produce isotactic polymers.

A series of cationic complexes [(ArN=CR-CR=NAr)PtMe(L)]⁺[BF₄]⁺ (Ar = aryl; R = H, CH₃; L = water, trifluoroethanol) has been prepared. They react smoothly with benzene at approximately room temperature in trifluoroethanol solvent to yield methane and the corresponding phenyl Pt(II) cations, via Pt(IV)-methyl-phenyl-hydride intermediates. The reaction products of methyl-substituted benzenes suggest an inherent reactivity preference for aromatic over benzylic C-H bond activation, which can however be overridden by steric effects. For the reaction of benzene with cationic Pt(II) complexes, in which the diimine ligands bear 3,5-disubstituted aryl groups at the nitrogen atoms, the rate-determining step is C-H bond activation. For the more sterically crowded analogs with 2,6-dimethyl-substituted aryl groups, benzene coordination becomes rate-determining. The more electron-rich the ligand, as reflected by the CO stretching frequency in the IR spectrum of the corresponding cationic carbonyl complex, the faster the rate of C-H bond activation. This finding, however, does not reflect the actual C-H bond activation process, but rather reflects only the relative ease of solvent molecules displacing water molecules to initiate the reaction. That is, the change in rates is mostly due to a ground state effect. Several lines of evidence suggest that associative substitution pathways operate to get the hydrocarbon substrate into, and out of, the coordination sphere; i.e., that benzene substitution proceeds by a solvent- (TFE-) assisted associative pathway.